Product Recalls in Pennsylvania

Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,792 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,792 in last 12 months

Showing 1468114700 of 29,947 recalls

Medical DeviceApril 3, 2019· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number:...

The Issue: Power Logic Board Fail Message on the 2008T BlueStar Machine with software...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceApril 3, 2019· Thommen Medical AG

Recalled Item: Adapter for handpiece Recalled by Thommen Medical AG Due to Dental adaptor...

The Issue: Dental adaptor does not conform to specifications. The dental coupling of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Becton Dickinson & Co.

Recalled Item: BD Veritor System Reader -In Vitro Diagnostic for use with Recalled by...

The Issue: Background calibration has the potential to cause false positive or false...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Becton Dickinson & Co.

Recalled Item: BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with Recalled...

The Issue: Background calibration has the potential to cause false positive or false...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Elekta Limited

Recalled Item: Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance...

The Issue: There is no warning in the Elekta Unity manual for the administration of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Randox Laboratories Ltd.

Recalled Item: G-6-PDH Normal Control (G-6-PDH CONTROL N) Recalled by Randox Laboratories...

The Issue: The target values and ranges in these lots are incorrect.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Randox Laboratories Ltd.

Recalled Item: G-6-PDH Deficient Control (G-6-PDH CONTROL D) Recalled by Randox...

The Issue: The target values and ranges in these lots are incorrect.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2019· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: Thermo Scientific General Purpose Dynamic Bath Precision 10L GP Bath...

The Issue: Product may have been assembled incorrectly,the assembly error can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2019· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: Fisher Scientific Isotemp -General Purpose Water Bath: lsotemp 20L GP...

The Issue: Product may have been assembled incorrectly,the assembly error can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2019· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: Fisher Scientific Isotemp -General Purpose Water Bath: lsotemp 10L GP...

The Issue: Product may have been assembled incorrectly,the assembly error can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2019· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: Fisher Scientific Isotemp -General Purpose Water Bath: lsotemp 5L GP...

The Issue: Product may have been assembled incorrectly,the assembly error can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2019· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: Thermo Scientific General Purpose Dynamic Bath Precision 5L GP Bath Recalled...

The Issue: Product may have been assembled incorrectly,the assembly error can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2019· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: Thermo Scientific General Purpose Dynamic Bath Precision 2L-Shallow GP Bath...

The Issue: Product may have been assembled incorrectly,the assembly error can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2019· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: Thermo Scientific General Purpose Dynamic Bath Precision 20L GP Bath...

The Issue: Product may have been assembled incorrectly,the assembly error can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2019· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: Thermo Scientific General Purpose Dynamic Bath Precision 28L GP Bath...

The Issue: Product may have been assembled incorrectly,the assembly error can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2019· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: Thermo Scientific General Purpose Dynamic Bath Precision 5 & 10L Recalled by...

The Issue: Product may have been assembled incorrectly,the assembly error can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Olympus Corporation of the Americas

Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...

The Issue: There is a potential for the single use suction valve to come apart and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Zimmer Biomet, Inc.

Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Incorrect part description contained on an additional label placed on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing